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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343534Erstellt: 24. Oktober 2026

Ethyl bromoacetate → 3-Cyano-3-(3,4-dimethylphenyl)pentanedioic acid diethyl ester

https://huagongshe.com/de/reaction/343534

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
Edukt2-(3,4-Dimethylphenyl)acetonitrileHCID 76401—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Cyano-3-(3,4-dimethylphenyl)pentanedioic acid diethyl esterHCID 53845428—

Reaktionsschritte

Cool a solution of sodium bis(trimethylsilyl)amide (723 mL, 1M in tetrahydrofuran, 723 mmol) to 0° C. in an ice bath. Add a solution of 3,4-dimethylphenylacetonitrile (50.0 mmol) in tetrahydrofuran (130 mL) over about 1.5 hours. When the addition is complete, warm the reaction mixture to ambient temperature and allow to stir. After 2 hours, transfer the above solution via cannula into a cooled (-50° C.) solution of ethyl bromoacetate (126 g, 757 mmol) in tetrahydrofuran (250 mL). After the transfer is complete, allow the reaction mixture to warm to ambient temperature. After 18 hours, dilute with diethyl ether (500 mL) and extract with water, 1M hydrochloric acid solution, saturated aqueous solution of sodium bicarbonate, and then brine. Dry the organic layer over MgSO4, filter, and concentrate in vacuo to give a residue. Recrystallize the residue from diethyl ether to give the title compound as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05861417
Quelldatensatzuspto-grants-1999_01
ORD IDord-def067296e584bd19a6a2ac04852f922
Quellennotizuspto-grants-1999_01